Single-molecule force spectroscopy of toehold-mediated strand displacement

Andreas Walbrun, Tianhe Wang, Michael Matthies, Petr Šulc, Friedrich C. Simmel () and Matthias Rief ()
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Andreas Walbrun: Center for Functional Protein Assemblies (CPA)
Tianhe Wang: Department of Bioscience
Michael Matthies: Department of Bioscience
Petr Šulc: Department of Bioscience
Friedrich C. Simmel: Department of Bioscience
Matthias Rief: Center for Functional Protein Assemblies (CPA)

Nature Communications, 2024, vol. 15, issue 1, 1-15

Abstract: Abstract Toehold-mediated strand displacement (TMSD) is extensively utilized in dynamic DNA nanotechnology and for a wide range of DNA or RNA-based reaction circuits. Investigation of TMSD kinetics typically relies on bulk fluorescence measurements providing effective, bulk-averaged reaction rates. Information on individual molecules or even base pairs is scarce. In this work, we explore the dynamics of strand displacement processes at the single-molecule level using single-molecule force spectroscopy with a microfluidics-enhanced optical trap supported by state-of-the-art coarse-grained simulations. By applying force, we can trigger and observe TMSD in real-time with microsecond and nanometer resolution. We find TMSD proceeds very rapidly under load with single step times of 1 µs. Tuning invasion efficiency by introducing mismatches allows studying thousands of forward/backward invasion events on a single molecule and analyze the kinetics of the invasion process. Extrapolation to zero force reveals single step times for DNA invading DNA four times faster than for RNA invading RNA. We also study the kinetics of DNA invading RNA, a process that in the absence of force would rarely occur. Our results reveal the importance of sequence effects for the TMSD process and have relevance for a wide range of applications in nucleic acid nanotechnology and synthetic biology.

Date: 2024
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DOI: 10.1038/s41467-024-51813-9

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